Recall StatusTerminated
Date Initiated2013-02-07
Date Terminated2017-04-20
Product QuantityUSA: 58 units, Foreign: 103 units
Reason for Recall
Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on some VITROS Systems may be
out of its manufacturing specifications. Extension springs are part of the slide alignment guide assembly. During an internal evaluation in its manufacturing facility, it was discovered that an extension spring had insufficient force. If the extension spring does not provide sufficient force, MicroSlides may not be properly positioned within the
MicroSlide incubator which has the potential to cause imprecise results. Extension springs are just one
component in the slide alignment assembly. OCD's evaluation determined that the probability of an out of
specification extension spring alone adversely affecting results is unlikely.
Firm Action
URGENT MEDICAL DEVICE CORRECTION letters were sent to the consignees on 2/07/13. On/about 2/07/13, OCD trained service personnel started to perform an assessment of all the VITROS System(s) in End-User facilities worldwide to determine if the extension springs are out of manufacturing specifications. In addition, the slide alignment guides will also be inspected. If the extension springs are out of specification they will be replaced. Consignees will also be provided with a communication that explains the issue.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwide Distribution- USA (nationwide) including Puerto Rico and countries of: Australia, Brazil, Canada, Chile, China, Colombia, England, France, Germany, India, Italy, Japan, Republic of Panama, Singapore, Spain, and Venezuela.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.